Successful Clinical Data Manager Lead with an 6 years experience in Pharma (MSD) and CRO (Icon, providing deliverables to Sanofi) I was working on studies in Therapeuric Areas such as Neurology, Oncology and Immunology and Inflammatory diseases. I have experience in InForm and Rave EDCs, I have experience with Oracle Clinical and Veeva Vault.
I was responsible for overseeing end-to-end data review and data delivery activities in clinical trials. I ensure that these activities are conducted on time, with high quality, and within agreed financial parameters. Their expertise includes a deep understanding of clinical data science, protocol content, and project management principles. I serve as the primary point of contact for internal and external stakeholders regarding data review activities and play a key role in forecasting resources required for data delivery.
Complete oversight of a given project or projects and is responsible for leading and coordinating the end-to-end quality deliverables of data management activities for clinical trials, including study set-up, conduct, and closeout. As CDSL I was also responsible for the execution of Data Management (DM) activities per set timelines with quality and consistency, and will provide comprehensive data management expertise and support to study team members cross-functionally.
The Associate Study Data Manager is responsible for routine data management activities during the course of a study under the supervision of study data manager, such as data review, validation, cleaning and tracking, as well as maintaining data management documents if needed
I was responsible for coordinating the end-to-end quality deliverables of data management activities for clinical trials, including study set-up, conduct, and close-out.
Primary point of contact for Clinical Data Management team in Poland, collaboration with Columbia Clinical Operations center and stakeholders, interim achievement, team lead role for data review in Poland.
Providing training to new hires, preparing to job certification.
Responsible for coordinating the end-to-end quality deliverables of data management activities for clinical trial including study set-up, conduct and close-out.